Costello Syndrome Latest Advances

Find the Latest Research About Costello Syndrome

Last Updated: 09/26/2026

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Found 632 publications

Content validity of the Familial Chylomicronemia Syndrome Symptoms and Impacts Scale (FCS-SIS) for severe hypertriglyceridemia (sHTG).

Content validity of the Familial Chylomicronemia Syndrome Symptoms and Impacts Scale (FCS-SIS) for severe hypertriglyceridemia (sHTG).

Journal: Patient related outcome measures
Published: September 04, 2026

Monogenic Familial Chylomicronemia Syndrome in Children: Clinical Divergences and Management Paradigms.

Monogenic Familial Chylomicronemia Syndrome in Children: Clinical Divergences and Management Paradigms.

Journal: Cureus
Published: August 05, 2026

Facial papillomatous thickening and strawberry-like gingival hyperplasia in Costello syndrome.

Facial papillomatous thickening and strawberry-like gingival hyperplasia in Costello syndrome.

Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: July 22, 2026

Olezarsen and Plozasiran: Novel apoC-III targeting medications for the treatment of hypertriglyceridemia.

Olezarsen and Plozasiran: Novel apoC-III targeting medications for the treatment of hypertriglyceridemia.

Journal: Journal of cardiovascular pharmacology
Published: July 06, 2026

Familial Chylomicronemia Syndrome Due to a Homozygous LPL c.644G>A Variant and Response to Volanesorsen in Colombia: A Case Report.

Familial Chylomicronemia Syndrome Due to a Homozygous LPL c.644G>A Variant and Response to Volanesorsen in Colombia: A Case Report.

Journal: Cureus
Published: June 21, 2026

Molecular characterization of individuals with RASopathies: Spectrum of genetic variants in a large Indian cohort.

Molecular characterization of individuals with RASopathies: Spectrum of genetic variants in a large Indian cohort.

Journal: Journal of genetics
Published: June 11, 2026

ApoC[III] You Later: A Review of Plozasiran for the Management of Familial Chylomicronemia Syndrome.

ApoC[III] You Later: A Review of Plozasiran for the Management of Familial Chylomicronemia Syndrome.

Journal: The Annals of pharmacotherapy
Published: June 06, 2026

Validation of two familial chylomicronemia syndrome clinical diagnosis scores in a cohort of molecularly defined patients.

Validation of two familial chylomicronemia syndrome clinical diagnosis scores in a cohort of molecularly defined patients.

Journal: Journal of clinical lipidology
Published: April 24, 2026

Clinical and Molecular Characterization of a RASopathy Cohort From Türkiye and an AMMECR1-Related Noonan Syndrome-Mimicking Phenotype.

Clinical and Molecular Characterization of a RASopathy Cohort From Türkiye and an AMMECR1-Related Noonan Syndrome-Mimicking Phenotype.

Journal: Clinical genetics
Published: April 15, 2026

Severe Familial Chylomicronemia Syndrome With Refractory Hypertriglyceridemia and Multisystem Complications Managed With Chronic Plasmapheresis and Olezarsen: A Case Report.

Severe Familial Chylomicronemia Syndrome With Refractory Hypertriglyceridemia and Multisystem Complications Managed With Chronic Plasmapheresis and Olezarsen: A Case Report.

Journal: Cureus
Published: March 20, 2026

Prevalence and clinical characteristics of probable familial chylomicronaemia syndrome at a tertiary care center in Pakistan: Insights from a hospital-based screening study.

Prevalence and clinical characteristics of probable familial chylomicronaemia syndrome at a tertiary care center in Pakistan: Insights from a hospital-based screening study.

Journal: Journal of clinical lipidology
Published: February 22, 2026

Utility of clinical scoring systems, laboratory, and genetic testing for appropriate classification of patients with severe hypertriglyceridemia in a Latin American cohort.

Utility of clinical scoring systems, laboratory, and genetic testing for appropriate classification of patients with severe hypertriglyceridemia in a Latin American cohort.

Journal: Journal of clinical lipidology
Published: February 13, 2026
Showing 1-12 of 632

Last Updated: 09/26/2026